A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979381



Internal ID20546421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35402104..35409956hg38UCSC Ensembl
chr10:35691032..35698884hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg387853
hg197853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443983
Supporting Variants
Samples
Known GenesCCNY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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